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FDA 510(k)

SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES

K-Number: K050183 · 2005-08-16

ApplicantSilvestrin Fabris S.R.L.
Decision Date2005-08-16
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Silvestrin Fabris S.R.L.. It received FDA 510(k) clearance on 2005-08-16 under 510(k) number K050183. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES?

SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES is a medical device that received FDA 510(k) clearance on 2005-08-16. The listed applicant is Silvestrin Fabris S.R.L.. The 510(k) number is K050183.

When did SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES receive FDA 510(k) clearance?

SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES received FDA 510(k) clearance on 2005-08-16, under 510(k) number K050183.

Who is the listed applicant for SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES?

The FDA 510(k) record lists Silvestrin Fabris S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES?

The FDA product code for SILFAB SUPER 2 MAX COMPRESSOR, N28 SERIES is CAF.

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Official Source

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